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Improving Service DeliveryThrough Access Points

This study has been completed.

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs
ClinicalTrials.gov Identifier: NCT00012623
  Purpose

CBOCs represent one of VA's main managed care strategies for shifting the focus of care from the inpatient to the outpatient setting and for improving the health of our nation's veterans. Hypothesis-driven research is critically needed to test the basic assumptions motivating the expansion of CBOCs throughout the VA health care system.


Condition
Hypertension
Angina
Diabetes

MedlinePlus related topics:   High Blood Pressure   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Retrospective
Official Title:   Improving Service DeliveryThrough Access Points

Further study details as provided by Department of Veterans Affairs:

Estimated Enrollment:   39481
Study Completion Date:   March 2002

Groups/Cohorts
1

Detailed Description:

Background:

CBOCs represent one of VA's main managed care strategies for shifting the focus of care from the inpatient to the outpatient setting and for improving the health of our nation's veterans. Hypothesis-driven research is critically needed to test the basic assumptions motivating the expansion of CBOCs throughout the VA health care system.

Objectives:

The purpose was to determine how increased geographic access to primary care services affects service use and costs. Two specific aims addressed were: 1) to determine how CBOCs impact the service use of all existing users and existing users with the following ambulatory care sensitive conditions (ACSC): alcohol dependence, angina, chronic obstructive pulmonary disease (COPD), depression, diabetes and hypertension; and 2) to describe how CBOCs affect the workload and costs of the VA health care system from the VISN's perspective.

Methods:

A quasi-experimental pre-post study design with intervention and reference groups was employed to compare service use and costs in the 18 months following the establishment of a new CBOC. Fifteen CBOCs from 11 VISNs were included in the analysis. For specific aim 1, the intervention group was defined as existing users in the catchment area of a new CBOC and the reference group was defined as matched existing users outside CBOC catchment areas. Multivariate statistical regression analyses were used to estimate the impact of residing within the CBOC catchment area on use and cost in the post-period, controlling for patient casemix and use/cost in the 18 month pre-period. For specific aim 2, the intervention group was defined as zip codes in the catchment area of a new CBOC and the reference group was defined as matched zip codes outside CBOC catchment areas. Average use and costs for all users, existing users and new users from intervention zip codes and reference zip codes were compared.

Status:

Complete.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

Subjects must live in the catchment area of a specified CBOC and have been diagnosed with a tracer condition.

Exclusion Criteria:

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00012623

Locations
United States, Arkansas
Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock    
      No. Little Rock, Arkansas, United States, 72114-1706

Sponsors and Collaborators

Investigators
Principal Investigator:     John C. Fortney, PhD     Central Arkansas VHS Eugene J. Towbin Healthcare Ctr, Little Rock    
  More Information


Publications of Results:

Responsible Party:   Department of Veterans Affairs ( Fortney, John - Principal Investigator )
Study ID Numbers:   ACC 97-068
First Received:   March 14, 2001
Last Updated:   August 14, 2008
ClinicalTrials.gov Identifier:   NCT00012623
Health Authority:   United States: Federal Government

Study placed in the following topic categories:
Vascular Diseases
Diabetes Mellitus
Angina Pectoris
Hypertension

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on October 10, 2008




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